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过去二十年非小细胞肺癌细胞凋亡领域被引用次数最多的100篇文章:一项文献计量学分析

Top 100 most-cited articles on apoptosis of non-small cell lung cancer over the past two decades: a bibliometrics analysis.

作者信息

Ma Leshi, Zhang Jing, Dai Zi, Liao Pei, Guan Jieshan, Luo Zhijie

机构信息

First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.

Department of Oncology, Chongqing Hospital, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Chongqing, China.

出版信息

Front Immunol. 2025 Jan 13;15:1512349. doi: 10.3389/fimmu.2024.1512349. eCollection 2024.


DOI:10.3389/fimmu.2024.1512349
PMID:39872524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11770037/
Abstract

BACKGROUND: Recently there has been an increasing number of studies have explored apoptosis mechanisms in lung cancer (LC). However, no researchers have conducted a bibliometric analysis of the most cited articles in this field. OBJECTIVE: To examine the top 100 most influential and cited publications on apoptosis in non-small cell lung cancer (NSCLC) from 2004 to 2023, summarizing research trends and key focus areas. METHODS: This study utilized the Web of Science Core Database (WOSCC) to research NSCLC apoptosis from 2004 to 2023, using keyword selection and manual screening for article searches. Bibliometrix package of R software 4.3.1 was used to generate distribution statistics for the top ten institutions, journals and authors. Citespace6.2. R6 was used to create the visualization maps for keyword co-occurrence and clustering. VOSviewer1.6.19 was used to conduct cluster analysis of publishing countries (regions), with data exported to SCImago Graphica for geographic visualization and cooperation analysis. VOSviewer1.6.19 was used to produced co-citation maps of institutions, journals, authors, and references. RESULTS: From 2004 to 2023, 13316 articles were retrieved, and the top 100 most cited were chosen. These were authored by 934 individuals from 269 institutions across 18 countries and appeared in 45 journals. Citations ranged from 150 to 1,389, with a median of 209.5. The most influential articles appeared in 2005 and 2007 (n=13). The leading countries (regions), institutions, journals and authors were identified as the United States (n=60), Harvard University (n=64), (n=15), SUN M and YANG JS (n=6). The top five keywords were "expression", "activation", "apoptosis", "pathway" and "gefitinib". This study indicates that enhancing apoptosis through circular RNA regulation and targeting the Nrf2 signaling pathway could become a key research focus in recent years. CONCLUSION: Apoptosis has been the subject of extensive research over many years, particularly in relation to its role in the pathogenesis, diagnosis, and treatment of NSCLC. This study aims to identify highly influential articles and forecast emerging research trends, thereby offering insights into novel therapeutic targets and strategies to overcome drug resistance. The findings are intended to serve as a valuable reference for scholars engaged in this field of study.

摘要

背景:近年来,越来越多的研究探讨了肺癌(LC)中的细胞凋亡机制。然而,尚无研究人员对该领域被引用次数最多的文章进行文献计量分析。 目的:研究2004年至2023年非小细胞肺癌(NSCLC)细胞凋亡方面最具影响力和被引用次数最多的前100篇出版物,总结研究趋势和重点关注领域。 方法:本研究利用Web of Science核心数据库(WOSCC)检索2004年至2023年NSCLC细胞凋亡相关文献,通过关键词选择和人工筛选进行文献检索。使用R软件4.3.1的Bibliometrix软件包生成前十机构、期刊和作者的分布统计数据。使用Citespace6.2.R6创建关键词共现和聚类的可视化图谱。使用VOSviewer1.6.19对发表国家(地区)进行聚类分析,将数据导出到SCImago Graphica进行地理可视化和合作分析。使用VOSviewer1.6.19生成机构、期刊、作者和参考文献的共被引图谱。 结果:2004年至2023年共检索到13316篇文章,选取了被引用次数最多的前100篇。这些文章由来自18个国家269个机构的934人撰写,发表在45种期刊上。被引用次数从150次到1389次不等,中位数为209.5次。最具影响力的文章发表于2005年和2007年(n = 13)。主要国家(地区)、机构、期刊和作者分别为美国(n = 60)、哈佛大学(n = 64)、(此处原文缺失信息)(n = 15)、孙M和杨JS(n = 6)。前五个关键词为“表达”“激活”“细胞凋亡”“途径”和“吉非替尼”。本研究表明,通过环状RNA调控增强细胞凋亡和靶向Nrf2信号通路可能成为近年来的关键研究重点。 结论:多年来,细胞凋亡一直是广泛研究的主题,尤其是在其与NSCLC发病机制、诊断和治疗的关系方面。本研究旨在识别高影响力文章并预测新兴研究趋势,从而为克服耐药性的新治疗靶点和策略提供见解。研究结果旨在为从事该研究领域的学者提供有价值的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/8fc6cc6d036a/fimmu-15-1512349-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/2072f15fdb9e/fimmu-15-1512349-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/8268c36b2a32/fimmu-15-1512349-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/04fcb477d5ed/fimmu-15-1512349-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/21a6df1d1dc5/fimmu-15-1512349-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/ec618543c9e4/fimmu-15-1512349-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/cdc5e1bbfc69/fimmu-15-1512349-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/6283002973fe/fimmu-15-1512349-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/f5743b676b0c/fimmu-15-1512349-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/4fdba03d046b/fimmu-15-1512349-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/24a33fc70c82/fimmu-15-1512349-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/8fc6cc6d036a/fimmu-15-1512349-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/2072f15fdb9e/fimmu-15-1512349-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/e445f8955ba7/fimmu-15-1512349-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/8268c36b2a32/fimmu-15-1512349-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/04fcb477d5ed/fimmu-15-1512349-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/21a6df1d1dc5/fimmu-15-1512349-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/ec618543c9e4/fimmu-15-1512349-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/cdc5e1bbfc69/fimmu-15-1512349-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/6283002973fe/fimmu-15-1512349-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/f5743b676b0c/fimmu-15-1512349-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/4fdba03d046b/fimmu-15-1512349-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/24a33fc70c82/fimmu-15-1512349-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5600/11770037/8fc6cc6d036a/fimmu-15-1512349-g012.jpg

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本文引用的文献

[1]
Comprehensive review of LncRNA-mediated therapeutic resistance in non-small cell lung cancer.

Cancer Cell Int. 2024-11-9

[2]
NRF2 Modulators of Plant Origin and Their Ability to Overcome Multidrug Resistance in Cancers.

Int J Mol Sci. 2024-10-26

[3]
lncRNAs'p potential roles in the pathogenesis of cancer via interacting with signaling pathways; special focus on lncRNA-mediated signaling dysregulation in lung cancer.

Med Oncol. 2024-11-8

[4]
Nrf2 in human cancers: biological significance and therapeutic potential.

Am J Cancer Res. 2024-8-25

[5]
NRF2 inhibitors: Recent progress, future design and therapeutic potential.

Eur J Med Chem. 2024-12-5

[6]
Integrative single-cell RNA-seq and spatial transcriptomics analyses reveal diverse apoptosis-related gene expression profiles in EGFR-mutated lung cancer.

Cell Death Dis. 2024-8-9

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New insights into the potential of exosomal circular RNAs in mediating cancer chemotherapy resistance and their clinical applications.

Biomed Pharmacother. 2024-8

[8]
Therapeutic targeting of apoptosis in chronic lymphocytic leukemia.

Semin Hematol. 2024-4

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Circular RNAs in the KRAS pathway: Emerging players in cancer progression.

Pathol Res Pract. 2024-4

[10]
Ameliorative inhibition of sirtuin 6 by imidazole derivative triggers oxidative stress-mediated apoptosis associated with Nrf2/Keap1 signaling in non-small cell lung cancer cell lines.

Front Pharmacol. 2024-1-3

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